The Von Willebrand’s disease or VWD is a blood disorder where the blood has a hard time clotting and cuts can bleed for a long time. Damage from the bleeding and the effect of it not clotting can affect the heart and other organs or can even cause death. Although death is possible from Von Willebrand’s disease it’s not a common issue. One of the main causes of death are because of a major injury and the body not being able to stop the bleeding.
If you have Von Willebrand’s disease it’s because the protein does not work the way it’s supposed to. This can be because of low amounts of particular proteins in the blood or because of a malfunction in the bloods makeup; the body will kick in to do what it has to do to survive.
When a normal healthy body gets an injury to the point that it causes the body to bleed small cell fragments will clot up to stop the bleeding. When this clotting starts it’s because of the platelets and the way they form together to stop the bleeding. People with Von Willebrand’s disease will not have the proper key factors in the blood to make the platelets stick together.
The Von Willebrand’s disease factor also carries clotting factor number 8 which is also the same protein that’s missing or not working properly with individuals who have been diagnosed with hemophilia. Von Willebrand’s disease is more likely to be present before some other blood disorders and is like a mild version of hemophilia.
There are 3 different types of this disorder and they are:
- Type 1 – The most common form of Von Willebrand’s disease
- Type 2 – Type 2 is divided into 4 different gene mutation 2A, 2B, 2N and 2M
- Type 3 – This is the most severe case and it’s very rare to have
The chances of a person having Von Willebrand’s disease are about 1 out of every 50 to 1000 people worldwide. One of the things about this blood disorder is that it affects both men and women unlike hemophilia which seem to mainly me in men.
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